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Change in Choroidal Thickness of Myopic Eyes With a Myopia Control Contact Lens

StatusEnrolling by Invitation
PhaseNot applicable
Started
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Record status
This record was last updated March 26, 2025 (before its estimated December 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Primary completion date: Feb 2025 to Dec 2025
    • Study completion date: Apr 2025 to Dec 2025
    v3
  2. Study description shortened, about 10 words
    • Study title expanded, about 8 words
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
In this study, the direct effect of the MiSight contact lens (Cooper Vision), a daily disposable contact lens recently approved in Germany for the treatment of myopia, will be investigated. The aim of this study is to demonstrate an increase in choroidal thickness due to the myopic defocus induced by the contact lens. The increase in choroidal thickness after 30 minutes of exposure to the myopic defocus induced by the contact lens will be demonstrated by measuring the subfoveal and macular choroidal thickness.
Trial Details
NCT Number NCT06636019
Lead Sponsor University Hospital Augsburg
Conditions
(from sponsor)		 Myopia
Related terms Myopia
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov